Contract Specialist

Our Site Contracts Team is growing rapidly, and we are currently seeking a full-time, office-based Contract Specialist to join our Site Contracts Team in France. This position plays a key role in the study start-up and clinical trial management processes at Medpace. As a Site Contract Specialist, you will have full responsibility for the life cycle of each contract through the preparation, negotiation, and finalization of contracts. If you want an exciting career where you use your previous expertise and can develop and grow your career even further within a global  environment, then this is the opportunity for you Responsibilities   Drafting, reviewing, negotiating, and finalizing agreements, termination letters or other legal documents required for a clinical study; Negotiate within client approved contract and budget templates and negotiation parameters; Identify and assesses legal, financial, and operational risks and escalate to appropriate Contract Lead or Contract Manager; Provide recommendations and alternative resolutions throughout negotiations using established escalation channels; Coordinate with internal  functional departments to ensure various site startup activities are aligned with contractual process and mutually agreed up timelines; and Keep up to date with applicable local regulations impacting clinical trial contracts.

Bachelor's degree; preferably in Law or Sciences. At least 1 year of relevant work experience; Prior contract negotiation experience preferred but not required; Strong attention to detail; and Full proficiency in French and strong English written and spoken communication skills. Please submit your CV in English. Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. Why Medpace? When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.   Purpose-Driven Work Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence   Collaborative Culture Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. Leadership throughout Medpace is both accessible and approachable   Continuous Growth & Development Office based environment with on-site mentors Defined career paths with clear advancement opportunities Industry renowned onboarding and training programs designed to accelerate professional development Ongoing training and continuous learning opportunities throughout your career An environment that encourages employees to influence change, contribute ideas, and grow quickly   Other Employee Benefits Competitive compensation programs that recognize and reward performance Comprehensive health, wellness, retirement, and PTO benefits Office based culture with occasional WFH that provides flexibility for eligible positions after training Company-sponsored social events    Please note benefits may vary based on country.      What to Expect Next A Medpace team member will review your application and if your profile matches our current